Canonical Allele Identifier: CA207979478
Gene:

Linked Data

dbSNP Id: rs188061531

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57722032G>A , CM000672.2:g.57722032G>A GRCh38
NC_000010.10:g.59481792G>A , CM000672.1:g.59481792G>A GRCh37
NC_000010.9:g.59151798G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.69-20647C>T
XR_001747454.1:n.86-20647C>T